Clinical Research Coordinator I

Rocky Mountain Cancer Centers; Boulder (CO); On-site; Full time

Job summary

A leading provider of cancer care is seeking a Clinical Research Coordinator I in Boulder to join a compassionate team dedicated to improving patient experiences. This role involves managing patient trials, data collection, and collaboration with medical professionals. Ideal candidates will possess relevant academic credentials and a passion for oncology research.

Benefits

Health, dental, and vision plans

401(k) retirement plan

Paid Time Off (PTO)

Tuition reimbursement

Potential for research bonus

Qualifications

• One year of clinical or scientific experience, preferably in Oncology.
• Previous Clinical Research Experience required.

Responsibilities

• Screen patients for protocol eligibility and presents trial details.
• Assists with patient care and regulatory document maintenance.
• Participates in data collection, entry, and reporting.

Skills

Communication

Organizational skills

Interpersonal skills

Attention to detail

Education

Associate's degree in a clinical or scientific related discipline

Bachelor's Degree Preferred

Tools

Microsoft Office

Job description

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Overview

Rocky Mountain Cancer Centers, Colorado's largest and most comprehensive

Overview

Rocky Mountain Cancer Centers, Colorado's largest and most comprehensive

provider of cancer care has an exciting opportunity for an experienced

Clinical Research Coordinator in Boulder.

Bring your established Oncology and or Research experience and join a team

dedicated to providing an excellent experience to patients.

We realize that it sounds cliche but it is true - taking care of cancer

patients is a calling. It's much more than a job. Each of us has a unique

story that brought us to Rocky Mountain Cancer Centers (RMCC), but those

stories usually share common themes of care, compassion, and commitment.

No matter the role each RMCC team member serves in, the goal is the same:

to provide the best care possible for each and every one of our patients.

Whether we are a nurse holding our patient's hand, or a scheduler on the

phone finding an appointment that fits into a patient's schedule, we are

deeply connected to our patients and do what we can to help.

If this sounds like you, we'd love to have you join our team.

Hourly range for CRC I Applicants: $25.00-$29.00

Pay is based on several factors including but not limited to education, work

experience, certification, etc. As of the date of this posting, in

addition to your salary, RMCC offers the following benefits for this

position, subject to eligibility requirements: Health, dental, and

vision plans; wellness program; health savings account; flexible

spending accounts; potential for research bonus depending on financials of

department after one year of employment; 401(k) retirement plan; life

insurance, short-term disability insurance; long-term disability

insurance, Employee Assistance Program; PTO, holiday pay, tuition

reimbursement, and employee paid critical illness and accident insurance.

Responsibilities

Screens potential patients for protocol eligibility. Presents trial concepts

and details to the patients, participates in the informed consent process,

and enrolls patients on clinical trials.

Assists with patient care in compliance with protocol requirements. May

disburse investigational drug and maintain investigational drug

accountability. Participates in data collection, entry, and reporting for

the subjects.

In collaboration with the physician, reviews patients for changes in

condition, adverse events, concomitant medication use, protocol

compliance, response to study drug and thoroughly documents all findings.

Participates in required training and education programs as well as monitoring

and auditing activities. May work directly with sponsors. May participate in

scheduling monitoring and auditing visits, as well as interact with the

monitors/auditors while onsite.

Assists with collection and maintenance of regulatory documents in accordance

with USOR SOPs and applicable regulations.

May assist in the packing and shipping of lab specimens to central vendors.

May be required to complete Hazmat and/or IATA training.

Qualifications

Associate's degree in a clinical or scientific related discipline

Required, Bachelor's Degree Preferred.

One year of experience in a clinical or scientific related discipline,

Preferably In Oncology Preferred. Previous Clinical Research Experience

required.

Business Experience -

Experience in Microsoft Office

Experience Working With Physicians Preferred

Specialized Knowledge/Skills -

Must have excellent communication skills

Excellent organizational skills

Strong ability to multi-task

Excellent time management skills

Must have strong interpersonal skills to be able to interact with multiple

people on many different levels

Must have a high level of attention to detail

Must be able to work in a fast-aced environment

May be responsible for basic clinical assessments

Working Conditions

The work environment characteristics described here are representative of

those an employee encounters while performing the essential functions of this

job. Reasonable accommodati ns will be offered to enable individuals with

Disabilities To Perform The Essential Functions. Exposure To Communicable

diseases, toxic substances, ionizing radiation, medical preparations and

other conditions common to an oncology/hematology clinic environment.

The physical demands described here are representative of those that must be

met by an employee to successfully perform the essential functions of this

job. Reasonable accommodations will be offered to enable individuals with

disabilities to perform the essential functions. Requires standing and walking

for extensive periods of time. Occasionally lifts and carries items weighing

up to 40 lbs. Requires corrected vision and hearing to normal range.

All qualified candidates are required to pass a background check and

non-federal drug test (which excludes marijuana) post offer of employment

and prior to hire.

We will be accepting applications on an ongoing basis for this position. To

apply for this position, start the process by clicking the blue "apply"

button.

The US Oncology Network is an Equal Opportunity Employer. All qualified

applicants will receive consideration for employment without regard to race,

color, religion, sex, national origin, sexual orientation, gender

identity, disability or protected veteran status.

Seniority level

• Seniority level

  Entry level

Employment type

• Employment type

  Full-time

Job function

• Job function

  Research, Analyst, and Information Technology

• Industries

  Hospitals and Health Care

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